Colon Cancer: Gene >> L1CAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153862821:153862821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3616G>A
AA Mutation	p.Asp1206Asn(p.D1206N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153863907:153863907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200798819
CDS Mutation	c.3433C>T
AA Mutation	p.Arg1145Cys(p.R1145C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153865124:153865124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2836G>A
AA Mutation	p.Gly946Ser(p.G946S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153864956:153864956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2911C>T
AA Mutation	p.Arg971Trp(p.R971W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153864417:153864417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781826722
CDS Mutation	c.3227C>T
AA Mutation	p.Thr1076Met(p.T1076M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153869631:153869631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Cys(p.R386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153868030:153868030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782196802
CDS Mutation	c.1796T>C
AA Mutation	p.Val599Ala(p.V599A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153872350:153872350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Cys(p.R68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153865750:153865750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201550159
CDS Mutation	c.2501G>A
AA Mutation	p.Arg834Gln(p.R834Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153870445:153870445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749G>A
AA Mutation	p.Ser250Asn(p.S250N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153864446:153864446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153865107:153865107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148187017
CDS Mutation	c.2853C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153868864:153868864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153865327:153865327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200799618
CDS Mutation	c.2721C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153872285:153872285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153871145:153871145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153870123:153870123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs797044787
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153867483:153867483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2010G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153862795:153862795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782341083
CDS Mutation	c.3642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370060
Start	153868074:153868074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201440831
CDS Mutation	c.1752C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000370060
Start	153868333:153868333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1672C>T
AA Mutation	p.Arg558Ter(p.R558*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000370060
Start	153869519:153869519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> L1CAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153870927:153870927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782070899
CDS Mutation	c.557C>T
AA Mutation	p.Thr186Met(p.T186M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153869631:153869631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Cys(p.R386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153864696:153864696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3055G>A
AA Mutation	p.Asp1019Asn(p.D1019N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153868319:153868319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1686G>T
AA Mutation	p.Glu562Asp(p.E562D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370060
Start	153868939:153868939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281G>T
AA Mutation	p.Lys427Asn(p.K427N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript